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SLC52A2 mutations cause SCABD2 phenotype: A second report.
Babanejad M, Adeli OA, Nikzat N, Beheshtian M, Azarafra H, Sadeghnia F, Mohseni M, Najmabadi H, Kahrizi K. Babanejad M, et al. Among authors: adeli oa. Int J Pediatr Otorhinolaryngol. 2018 Jan;104:195-199. doi: 10.1016/j.ijporl.2017.11.014. Epub 2017 Nov 20. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29287867
When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS).
Mohseni M, Akbari M, Booth KT, Babanejad M, Azaiez H, Ardalani F, Arzhangi S, Jalalvand K, Nikzat N, Ghodratpour F, Jamali P, Adeli OA, Habibi H, Kahrizi K, Najmabadi H. Mohseni M, et al. Among authors: adeli oa. J Hum Genet. 2020 Jul;65(7):609-617. doi: 10.1038/s10038-020-0740-z. Epub 2020 Mar 30. J Hum Genet. 2020. PMID: 32231217 Free PMC article.